Author:
Battelino Saba,Klancar Gasper,Kovac Jernej,Battelino Tadej,Trebusak Podkrajsek Katarina
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Otorhinolaryngology
Reference18 articles.
1. Morton CW, Nance E (2006) Newborn hearing screening––a silent revolution. N Engl J Med 354:2151–2164
2. Kenna MA, Feldman HA, Neault MW, Frangulov A, Wu BL, Fligor B, Rehm HL (2010) Audiologic phenotype and progression in GJB2 (Connexin 26) hearing loss. Arch Otolaryngol Head Neck Surg 136:81–87
3. Beck C, Pérez-Álvarez JC, Sigruener A, Haubner F, Seidler T, Aslanidis C et al (2014) Identification and genotype/phenotype correlation of mutations in a large German cohort with hearing loss. Eur Arch Otorhinolaryngol. doi: 10.1007/s00405-014-3157-5
4. Petersen MB, Willems PJ (2006) Non-syndromic, autosomal–recessive deafness. Clin Genet 69:371–392
5. Battellino S, Rudolf G, Zargi M, Podkrajsek KT, Peterlin B (2011) Connexin 26 (GJB2) and connexin 30 del(GJB6-D13S1830) mutations in Slovenians with prelingual non-syndromic deafness. Int Adv Otol 7:372–378
Cited by
23 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献